Creatinine measured in the blood is the most commonly measured endogenous filtration marker. It is a 113 Dalton amino acid derivative that is generated from the breakdown of creatinine in muscle, distributed throughout total body water, and excreted by the kidneys by glomerular filtration and tubular secretion. Although the blood level is affected primarily by the level of GFR, it is also affected by three other physiological processes (non-GFR determinants): generation by muscle mass and diet, tubular secretion by active transport, and extra-renal elimination by gastrointestinal or third space losses. Due to variation in these unmeasured processes, particularly creatinine generation, amongst individuals and within individuals over time, the normal values for creatinine differs among groups. The estimated GFR based on creatinine (eGFRcr) adjusted for demographic factors (age, sex and race) or clinical factors (weight and others) that are related to these processes, provides more information that the creatinine alone. All creatinine based estimating equations are limited by non-GFR determinants of creatinine that cannot be accounted for by the demographic and clinical factors. This is especially important in conditions associated with muscle wasting, as can be seen with severe acute or chronic illnesses.
The 2012 KDIGO CKD guidelines recommended the 2009 CKD-EPI creatinine equation as the first step in GFR evaluation. As of 2020, the three most commonly used equations are the 2009 CKD-EPI creatinine equation and the Modification of Diet in Renal Disease (MDRD) Study equation, which include age, sex and race, and Cockcroft and Gault equation, which includes age, sex and weight. In 2021, the NKF-ASN Task Force on Reassessing the Inclusion of Race in Diagnosing Kidney Diseases concluded that race should not be included in GFR estimating equations, and recommended use of the 2021 CKD-EPI creatinine equation that includes age and sex but not race.